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FRESENIUS ARTERIAL BLOODLINE SETS FOR HEMODIALYSIS, FRESENIUS COMBI SETS HEMODIALYSIS BLOOD TUBING SETS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012242
510(k) Type
Special
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2001
Days to Decision
30 days
Submission Type
Summary

FRESENIUS ARTERIAL BLOODLINE SETS FOR HEMODIALYSIS, FRESENIUS COMBI SETS HEMODIALYSIS BLOOD TUBING SETS

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012242
510(k) Type
Special
Applicant
Fresenius Medical Care North America
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/16/2001
Days to Decision
30 days
Submission Type
Summary